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聚合物微粒系统中包封效率和初始突释的控制

Control of encapsulation efficiency and initial burst in polymeric microparticle systems.

作者信息

Yeo Yoon, Park Kinam

机构信息

Purdue University, Department of Pharmaceutics, West Lafayette, IN 47907, USA.

出版信息

Arch Pharm Res. 2004 Jan;27(1):1-12. doi: 10.1007/BF02980037.

Abstract

Initial burst is one of the major challenges in protein-encapsulated microparticle systems. Since protein release during the initial stage depends mostly on the diffusional escape of the protein, major approaches to prevent the initial burst have focused on efficient encapsulation of the protein within the microparticles. For this reason, control of encapsulation efficiency and the extent of initial burst are based on common formulation parameters. The present article provides a literature review of the formulation parameters that are known to influence the two properties in the emulsion-solvent evaporation/extraction method. Physical and chemical properties of encapsulating polymers, solvent systems, polymer-drug interactions, and properties of the continuous phase are some of the influential variables. Most parameters affect encapsulation efficiency and initial burst by modifying solidification rate of the dispersed phase. In order to prevent many unfavorable events such as pore formation, drug loss, and drug migration that occur while the dispersed phase is in the semi-solid state, it is important to understand and optimize these variables.

摘要

初始突释是蛋白质包封微粒系统面临的主要挑战之一。由于初始阶段的蛋白质释放主要取决于蛋白质的扩散逸出,防止初始突释的主要方法集中在将蛋白质有效包封于微粒内。因此,包封效率和初始突释程度的控制基于常见的制剂参数。本文对乳液-溶剂蒸发/萃取法中已知会影响这两种性质的制剂参数进行了文献综述。包封聚合物的物理和化学性质、溶剂系统、聚合物-药物相互作用以及连续相的性质是一些有影响的变量。大多数参数通过改变分散相的固化速率来影响包封效率和初始突释。为了防止在分散相处于半固态时发生的许多不利事件,如孔隙形成、药物损失和药物迁移,了解并优化这些变量很重要。

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